Beijing Research Institute of Chinese Medicine, Beijing University of Chinese Medicine, Beijing 100013, China.
School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing 100013, China.
Molecules. 2024 Mar 19;29(6):1354. doi: 10.3390/molecules29061354.
The potential hepatotoxicity of Herba Epimedii is a focal point in traditional Chinese medicine security applications. As determined in our previous study, the flavonoid constituents of Herba Epimedii, sagittatoside A, icariside I, baohuoside I and icaritin, are related to the hepatotoxicity of this herb. However, the hepatotoxic mechanism of these components needs to be clarified further, and whether these components can maintain their injury action following liver metabolism needs to be confirmed. Herein, the effects of sagittatoside A, icariside I, baohuoside I and icaritin on the apoptosis of HepG2 cells and the expression of key proteins, including Bax, Bcl-2, Caspase-3 and Caspase-9, were evaluated. Moreover, with liver microsome incubation, the influences of metabolism on the apoptotic activities of these components were investigated. Then, by HPLC-MS/MS analyses, the in vitro metabolic stability of these components was determined after incubation with different kinds of liver microsomes to explain the reason for the influence. The results suggested that sagittatoside A, baohuoside I and icaritin could induce apoptosis, which is likely to be closely related to the induction of the intrinsic apoptosis pathway. After metabolic incubation, the sagittatoside A and icaritin metabolism mixture could still induce apoptosis due to less metabolic elimination, while the icariside I and baohuoside I metabolism mixtures respectively got and lost the ability to induce apoptosis, probably due to quick metabolism and metabolic transformation. The findings of this study may provide important references to explore the material basis and mechanism of the hepatotoxicity of Herba Epimedii.
中药淫羊藿的潜在肝毒性是其安全应用的一个焦点。在我们之前的研究中,淫羊藿的黄酮类成分,如朝藿定 A、朝藿定 C、宝藿苷 I 和淫羊藿苷,与该草药的肝毒性有关。然而,这些成分的肝毒性机制需要进一步阐明,并且需要确认这些成分在肝脏代谢后是否能保持其损伤作用。在此,评估了朝藿定 A、朝藿定 C、宝藿苷 I 和淫羊藿苷对 HepG2 细胞凋亡和关键蛋白(包括 Bax、Bcl-2、Caspase-3 和 Caspase-9)表达的影响。此外,通过肝微粒体孵育,研究了代谢对这些成分凋亡活性的影响。然后,通过 HPLC-MS/MS 分析,在不同种类的肝微粒体孵育后,测定这些成分的体外代谢稳定性,以解释影响的原因。结果表明,朝藿定 A、宝藿苷 I 和淫羊藿苷均可诱导细胞凋亡,这可能与诱导细胞内凋亡途径密切相关。经代谢孵育后,由于代谢消除较少,朝藿定 A 和淫羊藿苷的代谢混合物仍能诱导细胞凋亡,而朝藿定 C 和宝藿苷 I 的代谢混合物分别获得和失去了诱导细胞凋亡的能力,可能是由于快速代谢和代谢转化。本研究的结果可能为探索淫羊藿肝毒性的物质基础和机制提供重要参考。